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Correlation of circulating betatrophin concentrations with insulin secretion capacity, evaluated by glucagon stimulation tests
AIM: To investigate the relationship between plasma betatrophin concentrations and insulin secretion capacity in people with Type 2 diabetes. METHODS: Glucagon stimulation tests (1 mg) were performed in 70 people with Type 2 diabetes after an overnight fast. Plasma betatrophin concentrations were me...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024035/ https://www.ncbi.nlm.nih.gov/pubmed/25655786 http://dx.doi.org/10.1111/dme.12696 |
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author | Tokumoto, S. Hamamoto, Y. Fujimoto, K. Yamaguchi, E. Okamura, E. Honjo, S. Ikeda, H. Wada, Y. Hamasaki, A. Koshiyama, H. |
author_facet | Tokumoto, S. Hamamoto, Y. Fujimoto, K. Yamaguchi, E. Okamura, E. Honjo, S. Ikeda, H. Wada, Y. Hamasaki, A. Koshiyama, H. |
author_sort | Tokumoto, S. |
collection | PubMed |
description | AIM: To investigate the relationship between plasma betatrophin concentrations and insulin secretion capacity in people with Type 2 diabetes. METHODS: Glucagon stimulation tests (1 mg) were performed in 70 people with Type 2 diabetes after an overnight fast. Plasma betatrophin concentrations were measured using an enzyme‐linked immunosorbent assay. Insulin secretion capacity was evaluated by measuring increments of C‐peptide concentration in response to glucagon stimulation, and creatinine clearance was determined by comparing creatinine concentrations in serum and 24‐h urine samples. RESULTS: Plasma betatrophin concentrations were positively correlated with duration of Type 2 diabetes (r = 0.34, P = 0.003), and negatively correlated with increments of C‐peptide concentration (r = 0.37, P = 0.001) and creatinine clearance (r = 0.37, P = 0.001). The correlation with increments of C‐peptide concentration remained significant after adjustment for age and duration of Type 2 diabetes (r = 0.25, P = 0.037). Multivariate analysis identified age and increments of C‐peptide concentration as independent factors associated with plasma betatrophin levels. CONCLUSION: Plasma betatrophin levels inversely correlate with insulin secretion capacity, suggesting that betatrophin levels are regulated by insulin secretion capacity in humans. |
format | Online Article Text |
id | pubmed-5024035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50240352016-09-23 Correlation of circulating betatrophin concentrations with insulin secretion capacity, evaluated by glucagon stimulation tests Tokumoto, S. Hamamoto, Y. Fujimoto, K. Yamaguchi, E. Okamura, E. Honjo, S. Ikeda, H. Wada, Y. Hamasaki, A. Koshiyama, H. Diabet Med Research Articles AIM: To investigate the relationship between plasma betatrophin concentrations and insulin secretion capacity in people with Type 2 diabetes. METHODS: Glucagon stimulation tests (1 mg) were performed in 70 people with Type 2 diabetes after an overnight fast. Plasma betatrophin concentrations were measured using an enzyme‐linked immunosorbent assay. Insulin secretion capacity was evaluated by measuring increments of C‐peptide concentration in response to glucagon stimulation, and creatinine clearance was determined by comparing creatinine concentrations in serum and 24‐h urine samples. RESULTS: Plasma betatrophin concentrations were positively correlated with duration of Type 2 diabetes (r = 0.34, P = 0.003), and negatively correlated with increments of C‐peptide concentration (r = 0.37, P = 0.001) and creatinine clearance (r = 0.37, P = 0.001). The correlation with increments of C‐peptide concentration remained significant after adjustment for age and duration of Type 2 diabetes (r = 0.25, P = 0.037). Multivariate analysis identified age and increments of C‐peptide concentration as independent factors associated with plasma betatrophin levels. CONCLUSION: Plasma betatrophin levels inversely correlate with insulin secretion capacity, suggesting that betatrophin levels are regulated by insulin secretion capacity in humans. John Wiley and Sons Inc. 2015-02-05 2015-05 /pmc/articles/PMC5024035/ /pubmed/25655786 http://dx.doi.org/10.1111/dme.12696 Text en © 2015 The Authors. Diabetic Medicine published by John Wiley & Sons Ltd on behalf of Diabetes UK. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Tokumoto, S. Hamamoto, Y. Fujimoto, K. Yamaguchi, E. Okamura, E. Honjo, S. Ikeda, H. Wada, Y. Hamasaki, A. Koshiyama, H. Correlation of circulating betatrophin concentrations with insulin secretion capacity, evaluated by glucagon stimulation tests |
title | Correlation of circulating betatrophin concentrations with insulin secretion capacity, evaluated by glucagon stimulation tests |
title_full | Correlation of circulating betatrophin concentrations with insulin secretion capacity, evaluated by glucagon stimulation tests |
title_fullStr | Correlation of circulating betatrophin concentrations with insulin secretion capacity, evaluated by glucagon stimulation tests |
title_full_unstemmed | Correlation of circulating betatrophin concentrations with insulin secretion capacity, evaluated by glucagon stimulation tests |
title_short | Correlation of circulating betatrophin concentrations with insulin secretion capacity, evaluated by glucagon stimulation tests |
title_sort | correlation of circulating betatrophin concentrations with insulin secretion capacity, evaluated by glucagon stimulation tests |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024035/ https://www.ncbi.nlm.nih.gov/pubmed/25655786 http://dx.doi.org/10.1111/dme.12696 |
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